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Guidance
DNA Anti-Contamination – Forensic Medical
Examination in Sexual Assault Referral Centres
and Custodial Facilities
FSR-G-207
ISSUE 1
© Crown copyright 2016
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1. INTRODUCTION ......................................................................................................... 3
2. SCOPE ........................................................................................................................ 4
3. IMPLEMENTATION .................................................................................................... 4
4. MODIFICATION .......................................................................................................... 4
5. TERMINOLOGY .......................................................................................................... 4
6. ANTI-CONTAMINATION MEASURES (Codes section 19.2) ...................................... 5
7. PROFESSIONAL RESPONSIBILITY .......................................................................... 6
7.1 Personnel: Training and competence (Codes sections 17 and 18) ..................... 6
8. FACILITIES ................................................................................................................. 7
9. PACKAGING AND GENERAL CHEMICALS AND MATERIALS (Codes section 12) .. 9
9.2 Consumables ...................................................................................................... 9
9.3 Equipment ......................................................................................................... 10
9.4 Use of personal barrier / protective equipment (FSR-G-208 section 18.3.18-20)
.......................................................................................................................... 11
10. METHODS AND PROCEDURES .............................................................................. 12
11. DOCUMENTATION ................................................................................................... 13
11.1 Exhibit labelling ................................................................................................. 13
11.2 Note taking and record keeping (Codes section 15) ......................................... 13
11.3 Statements and reports (Codes section 25) ...................................................... 14
12. REVIEW .................................................................................................................... 14
13. ABBREVIATIONS ..................................................................................................... 14
14. REFERENCES .......................................................................................................... 15
15. GLOSSARY ............................................................................................................... 17
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1. INTRODUCTION
1.1.1 The purpose of this document is to provide guidance for the ‘forensic medical’
examination of persons.
1.1.2 This interim guidance sets out the Forensic Science Regulator’s minimum DNA
anti-contamination recommendations for the forensic medical examination of
persons examined in sexual assault referral centres (SARCs) or custodial
settings such as police custody suites.
1.1.3 All healthcare professionals (HCP) providing forensic science services including
evidential sample collection shall take due regard of the Forensic Science
Regulator’s Codes of Practice and Conduct for Providers and Practitioners in
the Criminal Justice System (the Codes)1 as it applies to them.
1.1.4 In the examination process the principle is to minimise the inadvertent transfer
of DNA material that could lead to the risk of a miscarriage of justice. This
includes the risk of wrongful conviction(s) or wrongful acquittal(s),obstructing or
delaying investigation(s).
1.1.5 There are potentially many routes by which contamination may occur; FSR-P-
302 (section1) provides further detail. By controlling the environment,
personnel, consumables and sampling procedures it is possible to minimise the
opportunities for contamination events; some example contamination routes are
provided in the table 1 below.
Direct transfer
Sample to Environment/item
Environment/item to Sample
Consumable to Sample
Person to Environment/item
Indirect transfer – secondary transfer
Environment/item to Examinee to Sample
Environment/item to Consumable to Sample
Environment/item to Practitioner to Sample
Environment/item to Environment/item to Sample
Person to Examinee to Sample
Person to Environment/item to Sample
Sample 1 to Environment/item to Sample 2
1 Forensic Science Regulator’s Codes of Practice and Conduct for Providers and Practitioners in the Criminal
Justice System. Available at: https://www.gov.uk/government/publications/forensic-science-providers-codes-of-practice-and-conduct-2016
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Indirect transfer – tertiary transfer
Person to Environment/item to Consumable to Sample
Person to Environment/item to Examinee to Sample
Environment/item to Environment/item to Examinee to Sample
Environment/item to Environment/item to Practitioner to Sample
Sample 1 to Environment/item to Examinee to Sample 2
Table 1: Examples of routes where contamination of DNA may occur
2. SCOPE
2.1.1 This guidance covers the minimum DNA anti-contamination practices and
processes for the taking of personal samples and recovery of other trace
evidence for forensic analysis from examinations, carried out in sexual assault
referral centres or custodial settings such as police custody suites.
3. IMPLEMENTATION
3.1.1 This guidance is available for incorporation into an organisation’s standard
practice, operating procedures and quality management system from the date
of publication and immediate implementation is strongly recommended. Full
compliance with the requirements set out in this guidance is expected by April
2017.
4. MODIFICATION
4.1.1 This is issued as interim guidance. Detailed requirements will be issued in due
course, therefore the status of some of the guidance may be changed from
good practice (should) to a mandatory requirement (shall/must).
5. TERMINOLOGY
5.1.1 The word ‘shall’2 has been used in this document where there is a
corresponding requirement in the Forensic Science Regulator’s Codes; the
word ‘should’3 has been used to indicate generally accepted practice where the
reason for not complying or any deviation shall be recorded.
2 In good medical practice ‘shall’ equates to ‘must’, which is used for an overriding duty or principle.
3 In good medical practice ‘should’ is used when providing an explanation of how to meet the overriding duty
and where the duty or principle will not apply in all situations or circumstances, or where there are factors
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6. ANTI-CONTAMINATION MEASURES (Codes section 19.2)
6.1.1 The Codes provide detailed requirements on contamination avoidance,
monitoring and detection; section 19.2.2 of the Codes describes steps to be
taken in establishing procedures relevant to contamination control.
6.1.2 From conducting a hazard or risk-based analysis (for example, process
mapping) with respect to contamination, the following conditions to prevent
cross-contamination should apply4.
a. The practitioner undertaking the forensic medical examination of a
complainant should not provide any medical examination or any other
service to the alleged suspect in the same case, for example, where the
suspect is in custody.
b. Where the provider of forensic medical practitioners delivers services to
both the SARC and custodial settings, there should be two separate rotas
in operation to ensure that the forensic medical practitioner available for
sexual offence forensic medical examinations of complainants is not used
for custody medicine at that time.
c. In the event that multiple complainants from the same crime attend the
SARC at the same time, or multiple suspects from the same alleged crime
are in custody at the same time, staff should ensure that they do not have
contact with multiple individuals linked to the same crime, in order to
prevent cross-contamination.
d. Police officers shall already have general forensic awareness training to
maintain and record separation of potentially conflicting or cross-
contaminating activities to ensure that suspects and complainants are
transported separately and that each individual is dealt with by different
outside the forensic practitioner/healthcare professional’s control that affect whether or how guidance can be followed. See the General Medial Council (GMC) Good Medical Practice Guide. 4 In exceptional circumstances (for example, very remote locations) where it becomes necessary to use the
same forensic practitioner/healthcare professional, the reason and rationale behind the decision and the steps that have been undertaken to reduce the risk of contamination shall be documented. For example, cleaning of mobile equipment including the outer surface of a medical bag; showering including hair wash; and a change of clothes shall be recorded and documented in the sexual assault referral centre (SARC) and/or custody record as appropriate and disclosed in any subsequent report or statement.
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staff5 If it becomes apparent that this practice has been breached then the
appropriate information shall be documented, brought to the attention of
the appropriate personnel and disclosed in any subsequent report or
statement.
7. PROFESSIONAL RESPONSIBILITY
7.1 Personnel: Training and competence (Codes sections 17 and 18)
7.1.1 The training and competency requirements set out in sections 17 and 18 of the
Codes should apply.
7.1.2 All healthcare professionals working in the police custodial setting or Sexual
Assault Referral Centres (SARC) should have undergone training and
assessment of competency6 7 in the forensic areas within which they are
working and should work within their competence. This includes personnel with
responsibility for the decontamination cleaning of the forensic areas of the
facility (for example, crisis worker).
7.1.3 Processes should be in place for assessing and maintaining on-going
competency, for example, this can include peer review, feedback on
environmental monitoring, samples taken, information provided to accompany
submissions for analysis and laboratory test results8 9.
5 See FSR 206 section 6.1.7-9, 6.1.20 and 6.2 for further information on DNA anti-contamination strategy.
6 ‘The UK Association of Forensic Nurses (UKAFN), College of Paramedics and Faculty of Forensic and
Legal Medicine (FFLM) have agreed that the minimum competency standard for all healthcare professionals (nurses, paramedics and doctors) working in the fields of general forensic medicine or sexual offence medicine should be either the UKAFN Advanced Standards in Education and Training (ASET) or the Licentiate of the Faculty of Forensic and Legal Medicine (LFFLM)’. http://www.fflm.ac.uk/2015/10/spress-release-doctors-nurses-and-paramedics-working-in-police-custody-call-for-standards-to-protect-patients-and-avoid-miscarriages-of-justice/ 7 The Faculty of Forensic and Legal Medicine has published standards for healthcare professionals (doctors,
nurses and paramedics) working in the these settings available at :
http://www.fflm.ac.uk/wp-content/uploads/2014/04/Quality-Standards-in-Forensic-Medicine-February-2016.pdf and http://www.fflm.ac.uk/wp-content/uploads/2016/06/Quality-Standards-for-Nurses-and-Paramedics-General-Forensic-Medicine-May-2016.pdf
8 Procedures to assess quality and feedback to the practitioner or service provider should be in place having
been developed collaboratively between the providers of forensic practitioners and the police.
9 Nittis, M., Stark, M. (2014) Evidence based practice: Laboratory feedback informs forensic specimen
collection in NSW.
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7.1.4 In addition to adhering to any professional requirements (for example, from the
Faculty of Forensic and Legal Medicine [FFLM], Royal College of Paediatrics
and Child Health [RCPCH] and college of paramedics) or regulatory
requirements (for example, from the General Medical Council [GMC] and
Nursing and Midwifery Council [NMC]), the code of conduct for forensic science
practitioners given on page 11 of the Codes shall be followed.
8. FACILITIES
8.1.1 As a minimum this guidance applies to any room or area used for receiving
persons for examination, medical examination and/or sample collection/storage.
8.1.2 There should be a named person within the facility with responsibility for
ensuring that a suitable environment is provided. This will enable the
practitioner to carry out their duties appropriately, without compromising the
integrity of any material or samples recovered. Any quality issues should be
reported to this named person10
Accommodation and environmental conditions (Codes sections 19.1, 19.2.3 and
23.3)
8.1.3 An identified room where the forensic medical examination or sample collection
will take place should be designated the ‘DNA clean’/‘forensic examination’ area
in readiness for use.
8.1.4 Walls, floors and furniture should be of smooth finish, sealed and resistant to
deterioration from frequent cleaning11.
8.1.5 Chairs should be height adjustable and shall be made or covered by non-
porous material such as vinyl, which can withstand frequent cleaning.
8.1.6 Drawer units should provide sufficient storage capacity to enable work surfaces
to be kept clear, other than for equipment in use.
8.1.7 There should be no strong air currents, notably from fans, vents or windows that
may be positioned near the examination, sampling and packaging areas. The
10 This should include informing the police forensic submissions/science unit.
11 Any new build post-October 2016 shall be required the meet the ideal practice as standard.
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management of cleaning, monitoring, handling and sampling procedures shall
take account of the risk of contamination (Codes 19.2.2a).
8.1.8 Decontamination (deep) cleaning of the whole forensic area using cleaning
agent(s) and method(s) demonstrated to be effective12 13 in removing levels of
DNA detected using routine profiling methods (Ballantyne et al., 2015) should
be carried out at least monthly to remove build-up of DNA contamination, see
FSR-G- 208 section 8.6)
8.1.9 Cleaning should be undertaken wearing sufficient barrier clothing (ibid., section
9.4) and glove management to prevent, as a minimum, transferring DNA from:
a. room and items to self;
b. self to room and items;
c. items to room;
d. items to items; and
e. room to room.
8.1.10 As a minimum, cleaning of high risk surfaces and equipment14 shall be
undertaken prior to each examination. In sexual assault referral centres
(SARCs), cleaning of high risk areas shall also be carried out after each
examination.
8.1.11 A record of the cleaning shall be maintained. As a minimum this should record
date, time and operator.
8.1.12 The number of persons accessing the medical examination room shall be
minimised by restricting access (Codes 19.2.3) to authorised personnel. The
documentation held shall record as a minimum, the date and time when each
client was examined, the practitioner(s) and any other persons in attendance.
12 National Institute of Justice Forensic Technology Center of Excellence, (2011) Comparison Study of
Disinfectants for Decontamination.
13 Examples of cleaning agents include 10% sodium hypochlorite (bleach, Presept™) solution, 1% Solution
Rely+On™ Virkon®, Microsol (10 %) and Distel (1%) (Trigene Advance).
14 These are surfaces and items that have a risk of transferring DNA directly to the examinee or to the
consumables used to recover and package samples and exhibits.
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8.1.13 There should be a programme of testing rooms, areas and/or equipment to
assess whether the decontamination policy is both effective and has been
carried out properly, i.e. environmental monitoring, see FSR-G-208 section 8.7).
9. PACKAGING AND GENERAL CHEMICALS AND MATERIALS (Codes
section 12)
9.1.1 Customers and providers shall ensure that any sample, packaging and/or
collection kits15 they use are fit for purpose.
9.1.2 Areas used for the storage and handling of consumables, samples and
exhibits16 shall be secure and access shall be restricted to authorised personnel
only (Codes 23.3).
Packaging
9.1.3 The packaging of collected material shall preserve the integrity of the potential
material for forensic examination and minimise the risk of loss, degradation or
contamination.
9.1.4 As a minimum this should include:
a. separate packaging of items where the packaging of items together is
likely to compromise them;
b. the appropriate packaging for the size, condition and forensic analysis
requirements of the material recovered; and
c. secure sealing.
9.2 Consumables
9.2.1 Consumables are single-use commodities used in the collection, preservation
and processing of material for forensic analysis, and are bought and used
routinely. These include barrier / personal protective equipment, tamper evident
15 This can be demonstrated by consumable manufacturers and kit assemblers meeting the requirements set
out for DNA consumables in BS ISO 18385:2016 Minimising the risk of human DNA contamination in products used to collect, store and analyse biological material for forensic purposes and for other non-DNA consumables in the publicly available specification (PAS) 377:2012 Specification for consumables used in the collection, preservation and processing of material for forensic analysis – Requirements for product, manufacturing and forensic kit assembly.
16 The requirements for drying cabinets and temporary storage areas are set out in FSR-G-206 section 10).
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containers, swabs, and packaging that comes into direct contact with the
material for forensic analysis. A consumable can also be equipment used in the
collection, processing and safe handling of the material, for example,
disposable tweezers or scissors.
9.2.2 Consumables utilised shall be such that they minimise the risk of DNA
contamination. As a minimum, sampling items such as swabs and water that
are declared as free from detectable human DNA17/’forensic DNA grade’18 shall
be used. A record of the batch/lot information shall be recorded.
9.2.3 Whether stored at the facility, in the examination room or carried by the
practitioner, as a minimum swabs, water ampoules, barrier clothing (suits,
aprons and sleeve covers), gloves and exhibit bags shall be protected from the
environment, either by outer protective packaging or packaged as part of a kit.
9.3 Equipment
9.3.1 Based on the risk assessment (Codes 19.2.2a) wherever possible the use of re-
usable equipment (for example, tweezers, scissors or pens) should be avoided.
9.3.2 Equipment that is not disposable and needs to be reused (for example,
colposcope, stethoscope, computer keyboards, mouse) shall be
decontaminated between each examination.
9.3.3 The cleaning agent(s) and method used shall be demonstrated to be effective in
removing detectable levels of DNA19 and do not interfere with downstream DNA
processing. A cleaning process example is as follows.
a. Items not suitable for immersion in fluid without being damaged should be
thoroughly cleaned using disposable cleaning roll or wipes liberally wetted
with a chemical that inactivates and removes DNA. If equipment will have
direct contact with sampling materials or has health and safety implications
17 Human DNA is not detectable by the most sensitive DNA profiling techniques available.
18 Demonstrated by compliance to BS ISO18385:2016 Minimising the risk of human DNA contamination in
products used to collect, store and analyse biological material for forensic purposes.
19 Examples of cleaning agents include 10% sodium hypochlorite (bleach, Presept™) solution, 1% Solution
Rely+On™ Virkon®, Ethanol (70% w/w) and Chlorhexadine Digluconate (2.5%w/w) wipes, Isopropyl Alcohol
(70%) wipes (Azo wipes), Microsol (10 %) and Distel (1%) (Trigene Advance).
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then the cleaning process should ensure that all residues of the cleaning
agent is removed, for example, by cleaning with sterile water. Where
equipment or items are susceptible to corrosion, then an appropriate
cleaning agent that does not corrode20 should be used.
b. Small items thought to be contaminated that are suitable for immersion in
fluid without damaging them should be submerged in a cleaning agent,
scrubbed/wiped down to remove material. If equipment will have direct
contact with sampling materials or has health and safety implications then
it should be rinsed in sterile distilled water and placed in clean sealed
protective packaging (for example, bag, plastic box) in readiness for the
next use.
9.4 Use of personal barrier / protective equipment (FSR-G-208 section 18.3.18-
20)
9.4.1 For the examination, persons who are not critical to the examination or support
of the victim should be excluded where possible, for example, police and family
members; all in attendance shall as a minimum wear protective barrier clothing
as defined below:
a. disposable barrier clothing to cover exposed/bare skin and the outer
clothing to prevent DNA transfer onto outer clothing, which is subsequently
transferred onto a handled item or another person, such as scrubs or
aprons and disposable sleeve covers;
b. non-latex powder free21 gloves (for example, nitrile).
It is also preferable for a mask and mob cap to be worn.
9.4.2 Hands shall be decontaminated before donning gloves, and following their
removal.
20 Activ8™ contains no oxidising or corrosive ingredients and can therefore be used with confidence on all
surfaces including fabrics and carpets. King’s College London and Metropolitan Police Service (2015) Cleaning project.
21 The powder in many types of gloves has been found to inhibit subsequent DNA analysis and can
potentially contaminate items being handled, therefore powdered gloves should be avoided.
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9.4.3 Double gloving with changes of the top gloves when handling different sample
sites, before handling equipment or after touching any other surfaces, such as
taps, door handles, bins, curtains, shall be employed.
9.4.4 For the cleaning activities, the following protective barrier clothing shall be worn
and put on in the following order:
a. face mask;
b. overshoes;
c. mob cap;
d. inner base gloves;
e. disposable lab coat, ‘scrubs’ scene suit or apron and sleeve covers; and
f. outer gloves.
9.4.5 Protective barrier clothing shall be changed after every forensic examination,
cleaning or maintenance task.
9.4.6 The protective barrier clothing shall be appropriately disposed of after use
(Codes 23.4).
10. METHODS AND PROCEDURES
10.1.1 Prior to using the examination room the forensic medical practitioner shall
satisfy themselves that adequate cleaning has taken place. If there is any doubt
as to the integrity of the cleanliness then in addition to the couch cover,
disposable sheeting shall be placed onto surfaces such as trolley, table, desks
to act as a barrier prior to use.
10.1.2 Any quality or integrity issue shall be brought to the attention of the centre or
appropriate facility manager and a record of the issue, date, time and to whom
the matter was reported shall be documented.
10.1.3 Following investigation it could require escalation to the Forensic Science
Regulator; examples are provided in the Codes section14.1.
10.1.4 A record of all persons in attendance at any time and the protective measures
taken during the examination shall be maintained.
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10.1.5 The Faculty of Forensic and Legal Medicine (FFLM) sampling guidelines
should be followed.
10.1.6 If required to use moistened swabs for sampling, then fresh clean gloves shall
be worn to open the water ampoule and the initial drops of water shall be
discarded as a means to flush the nozzle before wetting the swab; if the nozzle
makes contact with any contaminated surface then the water ampoule shall be
discarded.
10.1.7 All exhibit bags should be labelled and sealed before they are transported for
storage, either within the facility or at an agreed alternative storage facility. This
should be the responsibility and ownership of the practitioner collecting the
items (Codes 23.3).
10.1.8 Forensic medical practitioners are categorised as individuals who pose a high
risk for DNA contamination, see FSR-P-302 section 7.5 and as such shall
provide DNA samples for elimination purposes (Codes 19.2.5 and FSR-P-302).
11. DOCUMENTATION
11.1 Exhibit labelling
11.1.1 The packaging of all items shall be labelled so that it allows for the chain of
custody to be tracked. As a minimum, labelling shall include:
a. a unique identifier (for example, barcode or a combination of date/case
number/operator/consecutive numbering);
b. description of the item;
c. the person and/or location from which the item was collected.
d. the date and time that the item was collected;
e. the name or identifier of the person who collected the item.
11.2 Note taking and record keeping (Codes section 15)
11.2.1 Any decision made by the professional shall be recorded along with the reason
for making the decision. Where an expected course of action is not followed,
then the reason for doing so shall be documented in the record.
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11.2.2 Notes shall contain sufficient detail to enable the practitioner to generate a
statement, if required, at a later date.
11.3 Statements and reports (Codes section 25)
11.3.1 Due regard should be taken of the disclosure obligations and the requirements
set out in the Criminal Procedure Rules and Criminal Practice Directions
((Ministry of Justice) for experts. Though duties to the court of professional
witnesses and experts are similar, it should be borne in mind that the court can
deem an individual an expert to give an opinion based on their experience and
knowledge; in addition, opinion evidence may rely on the statements provided
by other practitioners22 Legal obligations are set out in FSR-I-400 and
disclosure requirements in the Association of Chief Police Officers (ACPO) and
the Crown Prosecution Service (CPS) guidance for experts.
12. REVIEW
12.1.1 The Forensic Science Regulator welcomes comments. Please send them to the
address as set out at: https://www.gov.uk/government/organisations/forensic-
science-regulator, or email: [email protected]
13. ABBREVIATIONS
Abbreviation Meaning
ACPO Association of Chief Police Officers, now replaced by the
National Police Chiefs’ Council (NPCC)
CoP College of Paramedics
CPS Crown Prosecution Service
DNA Deoxyribonucleic acid
FFLM Faculty of Forensic & Legal Medicine of the Royal College of
22 The forensic scientist may rely upon the statement from the forensic medical practitioner when evaluating
and forming an opinion of their scientific findings.
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Physicians
FSR Forensic Science Regulator
HCP Healthcare Professional
ISO International Organisation for Standardization
PPE personal protective equipment
SARC sexual assault referral centre
UKAFN United Kingdom Association of Forensic Nurses
14. REFERENCES
ACPO/CPS (2010) Guide Booklet for Experts May 2010. Available from:
http://www.cps.gov.uk/legal/d_to_g/disclosure_manual/annex_k_disclosure_ma
nual/index.html [Accessed 07/09/2014].
Ballantyne, K., Salemi, R., Guarino, F., Pearson, J., Garlepp, D., Fowler, S.
and van Oorschot, R. (2015) ‘DNA contamination minimisation – finding an
effective cleaning method’, Australian Journal of Forensic Sciences, vol. 47,
issue 4, pp 428–439.
British Standards (2016) BS ISO 18385:2016 Minimising the risk of human
DNA contamination in products used to collect, store and analyse biological
material for forensic purposes. Available from:
http://shop.bsigroup.com/ProductDetail/?pid=000000000030289935
Criminal Practice Directions. Available from:
https://www.judiciary.gov.uk/publications/criminal-practice-directions-2015/
[Accessed 07/12/15].
Criminal Procedure Rules Published by the Ministry of Justice on behalf of the
Criminal Procedure Rule Committee. London: Ministry of Justice. Available
from: http://www.legislation.gov.uk/uksi/2015/1490/contents/made [Accessed
07/12/15].
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Faculty of Forensic and Legal Medicine (2016) Quality Standards in Forensic
Medicine. Available from: http://www.fflm.ac.uk/wp-
content/uploads/2014/04/Quality-Standards-in-Forensic-Medicine-February-
2016.pdf [accessed 21/07/2016].
Faculty of Forensic and Legal Medicine (2016) Quality Standards for nurses
and paramedics. Available from: http://www.fflm.ac.uk/wp-
content/uploads/2016/06/Quality-Standards-for-Nurses-and-Paramedics-
General-Forensic-Medicine-May-2016.pdf [accessed 21/07/2016].
Faculty of Forensic and Legal Medicine (2016) Recommendations of
Collection of Specimens from Complainants and Suspects 2016. Available from:
http://www.fflm.ac.uk/publications/recommendations-for-the-collection-of-
forensic-specimens-from-complainants-and-suspects-3/ [Accessed 29/06/2016].
Forensic Science Regulator Codes of Practice and Conduct for Providers and
Practitioners in the Criminal Justice System. Birmingham: Forensic Science
Regulator. Available from: https://www.gov.uk/government/collections/forensic-
science-providers-codes-of-practice-and-conduct [Accessed 29/06/2016].
Forensic Science Regulator DNA contamination detection: The management
and use of staff elimination DNA databases, FSR-P-302. Birmingham: Forensic
Science Regulator. Available from:
https://www.gov.uk/government/publications/dna-contamination-detection
[Accessed 29/06/2016].
Forensic Science Regulator The control and avoidance of contamination in
crime scene examination involving DNA evidence recovery, FSR-G-206,
Forensic Science Regulator. Available from:
https://www.gov.uk/government/collections/dna-guidance [Accessed
13/07//2016].
Forensic Science Regulator Legal Obligations for Witnesses Providing expert
evidence, FSR-I-400. Birmingham: Forensic Science Regulator. Available from:
https://www.gov.uk/government/collections/fsr-legal-guidance [Accessed
29/06/2016].
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Forensic Science Regulator The control and avoidance of contamination in
laboratory activities, involving DNA evidence recovery and analysis, FSR-G-
208. Birmingham: Forensic Science Regulator. Available from:
https://www.gov.uk/government/publications/laboratory-dna-anti-
contamination-guidance [Accessed 29/06/2016].
General Medical Council ‘Good Medical Practice Guide’. Available from:
http://www.gmc-uk.org/guidance/good_medical_practice.asp [Accessed
29/06/2016].
King’s College London and Metropolitan Police Service (2015) Cleaning
project. Personal communication to the Forensic Science Regulator DNA
specialist group meeting. 10 July 2015.
National Institute of Justice Forensic Technology Center of Excellence,
(2011) Comparison Study of Disinfectants for Decontamination, Award No.
2010-DN-BX-K210. Available from: http://www.nfstc.org/wp-
content/files//Decontamination_Study_-_Revised_247.pdf [Accessed
13/07//2016].
Nittis, M., Stark, M. (2014) ‘Evidence based practice: Laboratory feedback
informs forensic specimen collection in NSW’, Journal of Forensic and Legal
Medicine, Vol. 25, pp38-44.
15. GLOSSARY
DNA clean area: Area in which appropriate DNA contamination prevention
measures should be maintained at all times.
DNA contamination: The introduction of DNA, or biological material containing
DNA, to an exhibit, or subsample derived from an exhibit during or after its
recovery from the scene of crime or a person. In the context of the Facility this
could occur for any of the following reasons.
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a. Poor practice23 employed by staff using fixtures and fittings and/or
collecting forensic samples.
b. DNA contamination from anybody who has had access to the forensic
waiting room and/or the medical examination room. Here key risk groups
are people from whom elimination DNA profiles have not been taken and
included in an elimination database (FSR-P-302), and therefore may be
inadvertently associated with a crime rather than being identified as
contamination. These may include visitors, contractors and people
accompanying a complainant into the forensic waiting room and/or the
medical examination room.
c. Insufficient use of cleaning regimes, or ineffective cleaning reagents used,
as part of a general forensic clean or a subsequent deep clean.
d. Residual DNA from the manufacture/maintenance of fixtures and fittings
that have not been deep cleaned.
Consumables: Single-use commodities used in the collection, preservation and
processing of material for forensic analysis, which are bought and used up
recurrently. These include personal protective equipment, tamper evident
containers, swabs, and packaging that come into direct contact with the material
for forensic analysis. A consumable can also be equipment used in the
collection, processing and safe handling of the material, for example,
disposable tweezers and scissors.
Facility: For the purpose of this document, this includes any room or area used
for receiving persons for examination, medical examination and/or sample
collection/storage.
Forensic DNA grade: Consumables certified to having met the requirements in
BS ISO 18385:2016.
Human DNA free: Human DNA is not detectable by the most sensitive DNA
profiling techniques available.
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It should be noted that even good practice does not eliminate the risk of contamination; it only helps to minimise it.
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Personal Protective Equipment (PPE): Items, for example, clothing and
gloves, which are used to prevent skin and mucous membrane exposure when
in contact with blood and body fluid on or from any complainant. PPE is also
worn to protect the practitioner from contact with harmful chemicals, for
example, during decontamination, and to minimise the chance that the wearer
causes inadvertent DNA contamination.
Practitioner: For the purpose of this document, the term is used to describe
personnel involved in the recovery of material for forensic analysis, including
those who are responsible for cleaning and DNA contamination, for example,
forensic physicians, forensic nurses, paramedics and crisis workers, i.e. all
appropriate healthcare professionals.
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Published by:
The Forensic Science Regulator
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Colmore Row
Birmingham
B3 2PW
https://www.gov.uk/government/organisations/forensic-science-regulator
ISBN: 978-1-78655-154-2